Relevance of tumour-infiltrating lymphocytes, PD-1 and PD-L1 in patients with high-risk, nodal-metastasised breast cancer of the German Adjuvant Intergroup Node-positive study.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
06 2019
Historique:
received: 07 02 2019
revised: 02 04 2019
accepted: 07 04 2019
pubmed: 11 5 2019
medline: 30 5 2020
entrez: 11 5 2019
Statut: ppublish

Résumé

Immune cell infiltration in breast cancer is important for the patient's prognosis and response to systemic therapies including immunotherapy. We sought to investigate the prevalence of tumour-infiltrating lymphocytes (TILs) and their association with immune checkpoints such as programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) in high-risk, node-positive breast cancer of the adjuvant German Adjuvant Intergroup Node-positive (GAIN-1) trial. We evaluated TILs by haematoxylin and eosin staining and PD-1 and PD-L1 (SP263 assay) expression by immunohistochemistry in 1318 formalin-fixed, paraffin-embedded breast carcinomas. The association of TILs with PD-1, PD-L1, molecular intrinsic subtypes, outcome and therapy regimens (dose-dense [dd] epirubicin, paclitaxel and cyclophosphamide [EPC] and dd epirubicin, cyclophosphamide, paclitaxel and capecitabine [EC-PwX]) was statistically tested. Overall TILs density was significantly associated with the expression of PD-1 and PD-L1 in immune cells (each p < 0.0001) and PD-L1 in tumour cells (p = 0.0051). TILs were more common in triple-negative breast cancer (TNBC) and human epidermal growth factor receptor 2 (HER2)-positive tumours (each p < 0.0001). On multivariate Cox regression analyses, patients with breast cancer without TILs had an unfavourable disease-free survival (DFS) in the EPC arm compared with the EC-PwX arm (hazard ratio [HR] = 0.69 [0.44-1.06], p = 0.0915); but no differences were seen in tumours with TILs (HR = 1.24 [0.92-1.67], p = 0.1566, interaction p = 0.0336). PD-1-positive immune cells in TNBC were associated with a significantly better DFS (HR = 0.50 [0.25-0.99], p = 0.0457). PD-L1 expression had no impact on patient outcome. TILs predict the benefit of intensified ddEPC compared with ddEC-PwX therapy in node-positive, high-risk breast cancer. TILs, PD-1 and PD-L1 are linked to each other indicating tumour immunogenicity. Moreover, PD-1-positive immune cells have a positive prognostic impact in TNBC. NCT00196872.

Sections du résumé

BACKGROUND
Immune cell infiltration in breast cancer is important for the patient's prognosis and response to systemic therapies including immunotherapy. We sought to investigate the prevalence of tumour-infiltrating lymphocytes (TILs) and their association with immune checkpoints such as programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) in high-risk, node-positive breast cancer of the adjuvant German Adjuvant Intergroup Node-positive (GAIN-1) trial.
PATIENTS AND METHODS
We evaluated TILs by haematoxylin and eosin staining and PD-1 and PD-L1 (SP263 assay) expression by immunohistochemistry in 1318 formalin-fixed, paraffin-embedded breast carcinomas. The association of TILs with PD-1, PD-L1, molecular intrinsic subtypes, outcome and therapy regimens (dose-dense [dd] epirubicin, paclitaxel and cyclophosphamide [EPC] and dd epirubicin, cyclophosphamide, paclitaxel and capecitabine [EC-PwX]) was statistically tested.
RESULTS
Overall TILs density was significantly associated with the expression of PD-1 and PD-L1 in immune cells (each p < 0.0001) and PD-L1 in tumour cells (p = 0.0051). TILs were more common in triple-negative breast cancer (TNBC) and human epidermal growth factor receptor 2 (HER2)-positive tumours (each p < 0.0001). On multivariate Cox regression analyses, patients with breast cancer without TILs had an unfavourable disease-free survival (DFS) in the EPC arm compared with the EC-PwX arm (hazard ratio [HR] = 0.69 [0.44-1.06], p = 0.0915); but no differences were seen in tumours with TILs (HR = 1.24 [0.92-1.67], p = 0.1566, interaction p = 0.0336). PD-1-positive immune cells in TNBC were associated with a significantly better DFS (HR = 0.50 [0.25-0.99], p = 0.0457). PD-L1 expression had no impact on patient outcome.
CONCLUSIONS
TILs predict the benefit of intensified ddEPC compared with ddEC-PwX therapy in node-positive, high-risk breast cancer. TILs, PD-1 and PD-L1 are linked to each other indicating tumour immunogenicity. Moreover, PD-1-positive immune cells have a positive prognostic impact in TNBC.
CLINICAL TRIAL
NCT00196872.

Identifiants

pubmed: 31075727
pii: S0959-8049(19)30246-1
doi: 10.1016/j.ejca.2019.04.010
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Programmed Cell Death 1 Receptor 0

Banques de données

ClinicalTrials.gov
['NCT00196872']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

76-88

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Aurelia Noske (A)

Institute of Pathology, Technical University of Munich, School of Medicine, Germany. Electronic address: a.noske@medica.ch.

Volker Möbus (V)

Department of Gynecology and Obstetrics, Hospital Frankfurt Höchst, Academic Hospital of the University Frankfurt, Germany.

Karsten Weber (K)

German Breast Group (GBG), Neu-Isenburg, Germany.

Sabine Schmatloch (S)

Breast Unit, Elisabeth-Krankenhaus Kassel, Kassel, Germany.

Wilko Weichert (W)

Institute of Pathology, Technical University of Munich, School of Medicine, Germany; German Cancer Consortium (DKTK), Partner Site Munich, Germany.

Claus-Henning Köhne (CH)

Department of Oncology, University Hospital Oldenburg, Oldenburg, Germany.

Christine Solbach (C)

Department of Gynecology and Obstetrics, University Hospital Frankfurt, Germany.

Barbara Ingold Heppner (B)

Institute of Pathology, Charité University Hospital, Berlin, Germany; Institute of Pathology, DRK Kliniken Berlin, Germany.

Katja Steiger (K)

Institute of Pathology, Technical University of Munich, School of Medicine, Germany; German Cancer Consortium (DKTK), Partner Site Munich, Germany.

Volkmar Müller (V)

Department of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Peter Fasching (P)

Department of Gynecology and Obstetrics, University Hospital Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany.

Thomas Karn (T)

Department of Gynecology and Obstetrics, University Hospital Frankfurt, Germany.

Marion van Mackelenbergh (M)

University Hospital Schleswig-Holstein, Kiel, Germany.

Frederik Marmé (F)

Department of Gynecology and National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Wolfgang D Schmitt (WD)

Institute of Pathology, Charité University Hospital, Berlin, Germany.

Christian Schem (C)

Breast Unit Krankenhaus Jerusalem, Hamburg, Germany.

Elmar Stickeler (E)

Department of Gynecology and Obstetrics, RWTH Aachen, Germany.

Sybille Loibl (S)

German Breast Group (GBG), Neu-Isenburg, Germany.

Carsten Denkert (C)

Institute of Pathology, Charité University Hospital, Berlin, Germany; Institute of Pathology, Philipps-University Marburg, Germany; German Cancer Consortium (DKTK), Partner Site Charité, Berlin, Germany.

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